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首页> 外文期刊>Applied and Environmental Microbiology >Analysis of Tox5 gene expression in Gibberella pulicaris strains with different trichothecene production phenotypes.
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Analysis of Tox5 gene expression in Gibberella pulicaris strains with different trichothecene production phenotypes.

机译:分析具有不同单端孢菌素生产表型的短赤霉菌中Tox5基因的表达。

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The Tox5 gene encodes trichodiene synthase, the first unique enzyme in the trichothecene biosynthetic pathway. In Gibberella pulicaris R-6380, the level of Tox5 mRNA was found to increase 47-fold in early stationary phase. Sequence analysis of the Tox5 promoter regions from geographically distinct strains of G. pulicaris revealed the existence of two Tox5 alleles (Tox5-1 and Tox5-2). All G. pulicaris strains that produce high levels of trichothecenes in liquid culture carry a 42-nucleotide (nt) tandem repeat sequence (Tox5-1) in the Tox5 promoter region, whereas strains that produce low levels of trichothecenes carry a single copy of this sequence (Tox5-2). A genetic cross between high- and low-level trichothecene producers resulted in the cosegregation of higher-level trichothecene production with the Tox5-1 allele. To determine the importance of the 42-nt repeat sequence in the regulation of Tox5 expression, reporter gene constructs carrying either the Tox5-1 or the Tox5-2 promoter region fused to the beta-galactosidase gene of Escherichia coli were introduced into the high-level-trichothecene-producing strain, R-6380. Expression of reporter gene activity in transformants was found to be regulated in a manner similar to Tox5 expression but appeared to be independent of the 42-nt sequence copy number. These results indicate that transcriptional controls play an important role in the regulation of Tox5 expression and that genes involved in trichothecene biosynthesis in G. pulicaris may be linked to Tox5.
机译:Tox5基因编码单端孢菌烯生物合成途径中的第一个独特的酶,单端孢菌烯合酶。在短赤霉R-6380中,发现Tox5 mRNA的水平在早期静止期增加了47倍。对来自G. pulicaris地理上不同菌株的Tox5启动子区域进行序列分析,发现存在两个Tox5等位基因(Tox5-1和Tox5-2)。所有在液体培养物中产生高水平单端孢菌丝菌的G. pulicaris菌株在Tox5启动子区域带有一个42核苷酸(nt)串联重复序列(Tox5-1),而低水平的单端孢菌丝菌菌株携带此单拷贝。顺序(Tox5-2)。高水平的单端孢菌素生产者之间的遗传杂交导致高水平的单端孢菌素生产者与Tox5-1等位基因共分离。为了确定42-nt重复序列在Tox5表达调控中的重要性,将携带与大肠杆菌β-半乳糖苷酶基因融合的Tox5-1或Tox5-2启动子区域的报告基因构建体引入到高级别三茂茂生产菌株,R-6380。发现转化子中报道基因活性的表达以类似于Tox5表达的方式被调节,但是似乎独立于42-nt序列拷贝数。这些结果表明,转录控制在Tox5表达的调节中起着重要作用,而参与G. pulicaris中单端孢菌素生物合成的基因可能与Tox5相关。

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